Identity
- Trade Name
- Six Panel PreScreen Plus Dip Card (CLIA Waived) FDA UDI
- Generic Name
- Multiple drugs of abuse IVD, kit, rapid ICT, clinical FDA UDI
- Device Name
- Six Panel PreScreen Plus Dip Card (CLIA Waived) Drug Combo: COC|AMP|MET|THC|OPI|PCP FDA UDI
- Model / Reference
- PS-DOA-164 FDA UDI
- Description
- Six Panel PreScreen Plus Dip Card (CLIA Waived) Drug Combo: COC|AMP|MET|THC|OPI|PCP FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00851000007151 FDA UDI
- FDA Product Code
- LCM FDA UDIDJG FDA UDILDJ FDA UDILAF FDA UDIDKZ FDA UDIDIO FDA UDI
- GMDN Term
- Multiple drugs of abuse IVD, kit, rapid ICT, clinical FDA UDI
Classification
- Device Class
- U FDA UDI
- Regulation Number
- 862.3650 FDA UDI862.3870 FDA UDI862.3610 FDA UDI862.3100 FDA UDI862.3250 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Multiple drugs of abuse IVD, kit, rapid ICT, clinical
Six Panel PreScreen Plus Dip Card (CLIA Waived) by Mergers Marketing, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class U | Pending data |
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Manufacturer
- Manufacturer
- Mergers Marketing, Inc.
Sources (1)
- FDA UDI 95976e32-7343-4d35-bdc9-7bf81619c352 33 fields · synced May 30, 2026